Dealing with iron: Common structural principles in proteins that transport iron and heme

被引:196
作者
Baker, HM
Anderson, BF
Baker, EN
机构
[1] Univ Auckland, Sch Biol Sci, Auckland 1, New Zealand
[2] Univ Auckland, Dept Chem, Auckland 1, New Zealand
[3] Massey Univ, Inst Mol Biosci, Palmerston North, New Zealand
关键词
D O I
10.1073/pnas.0637295100
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Iron is essential to life, but poses severe problems because of its toxicity and the insolubility of hydrated ferric ions at neutral pH. In animals, a family of proteins called transferrins are responsible for the sequestration, transport, and distribution of free iron. Comparison of the structure and function of transferrins with a completely unrelated protein hemopexin, which carries out the same function for heme, identifies molecular features that contribute to a successful protein system for iron acquisition, transport, and release. These include a two-domain protein structure with flexible hinges that allow these domains to enclose the bound ligand and provide suitable chemistry for stable binding and an appropriate trigger for release.
引用
收藏
页码:3579 / 3583
页数:5
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